Bioprocess Associate — GMP Manufacturing & Ops

Bristol Myers Squibb

Harvard (MA)

On-site

USD 34,000 - 43,000

Full time

14 days+

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Benefits offered by this job

Health Coverage
Wellbeing Support
Financial Well-being

Job summary

Bristol Myers Squibb’s Devens, MA site seeks a Bioprocess Associate to assist in manufacturing of therapeutic proteins under cGMPs. You will perform routine tasks, maintain clean-room standards, and support process automation and SAP workflows.

Training includes bioreactors, chromatography skids, media preparation, and related systems. The role requires a high school diploma; a BS in science/engineering/biochemistry or related field is preferred.

Qualifications

  • High school diploma required; B.S. in science/engineering/biochemistry or related field desired but not required.
  • Strong teamwork and collaboration experience from work/study.
  • Proficiency with word processing, spreadsheets, and web-based apps; attention to detail and accountability.
  • Good interpersonal skills and ability to maintain professional relationships with management and co-workers.

Responsibilities

  • Performs routine manufacturing tasks per written procedures and recognizes deviations.
  • Adheres to cGMPs and standard operating procedures.
  • Weighs, checks materials; assembles, cleans, and sterilizes process equipment; monitors processes.
  • Completes electronic work instructions and maintains clean-room conditions to meet regulatory standards.
  • Trains in bioreactor, chromatography skids, and media/buffer prep equipment; trains in process automation systems (Delta V, Syncade, Pi Vision) and business systems (SAP, Infinity, Maximo).
  • Assists in revising/creating process documents (SOPs, eWIs).
  • Maintains inventory levels of materials and components.
  • Supports a safe work environment.

Education

B.S. in science/engineering/biochemistry or related discipline

Tools

SAP
Infinity
Maximo

Job description

Bristol Myers Squibb’s Devens, MA site seeks a Bioprocess Associate to assist in manufacturing of therapeutic proteins under cGMPs. You will perform routine tasks, maintain clean-room standards, and support process automation and SAP workflows.

Training includes bioreactors, chromatography skids, media preparation, and related systems. The role requires a high school diploma; a BS in science/engineering/biochemistry or related field is preferred.

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